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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Ozone Concentration versus Temperature: Atmospheric Aging of Soot Particles
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Ozone Concentration versus Temperature: Atmospheric Aging of Soot Particles

机译:臭氧浓度与温度:烟灰粒子的大气老化

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The oxidation of soot particles with ozone (O-3) increases the particles' ability to act as cloud condensation nuclei (CCN). To assess if this process is a relevant source for CCN in the atmosphere, the reaction rate at atmospheric conditions must be known. Here we investigate the increase in CCN activity of soot particles rich in organic carbon at O-3 concentrations ranging from 0-200 ppb and between 5 and 35 degrees C. We operated an similar to 3 m(3) aerosol chamber as a continuous-flow stirred tank reactor which allows for aging times of up to 12 h and beyond and of particle size selection prior to the aging step. We applied the activation time (t(act)) concept to retrieve kinetic data. It was found that 100 nm soot particles can be CCN-active down to supersaturations of 0.3% after 12 h of exposure to 200 ppb O-3 at 35 degrees C. The reaction rate was found to be not directly proportional to the O-3 concentration. Instead, a Langmuir-type reaction kinetic was found to be the best fit to parametrize the reaction rates. The initial reaction step is therefore the adsorption of O-3 molecules, which could be detected by an increase in the particle diameter of up to 3.7 nm within several minutes after exposure. The increase in particle diameter agrees well with the calculated change in the O-3 surface coverage, which was obtained from CCN activation data under the assumption of a Langmuir-sorption isotherm. Further, we found that a temperature increase from 5 to 35 degrees C increases the reaction rate by a factor of 5 which corresponds to an activation energy of 38.5 kJ.mol(-1). Extrapolation to atmospheric conditions allows for the conclusion that the temperature is as important as the O-3 concentration for the CCN activation of soot particles within the atmospheric range.
机译:具有臭氧(O-3)的烟灰颗粒的氧化增加了颗粒充当云凝结核(CCN)的能力。为了评估该过程是大气中CCN的相关源,必须知道大气条件下的反应速率。在这里,我们研究富含0-200ppb浓度富含0-200ppb和5-35℃的烟灰颗粒的CCN活性的增加。我们将类似于3米(3)个气溶胶室作为连续的 - 流动搅拌釜反应器,其在老化步骤之前允许在老化时间和粒度选择的老化时间和粒度选择。我们应用了激活时间(T(ACT))概念来检索动态数据。结果发现,在35℃下暴露于200ppb O-3的12小时后,100nm烟灰颗粒可以是0.3%的超饱和0.3%。发现反应速率与O-3的反应速度不正常成比例专注。相反,发现Langmuir型反应动力学是最适合参数化反应速率的。因此,初始反应步骤因此吸附O-3分子,其可以在暴露后几分钟内的几分钟内的粒径增加至3.7nm的粒径。粒径的增加与计算出的O-3表面覆盖的变化吻合良好,这是在朗米尔吸附等温线的假设下从CCN活化数据获得的。此外,我们发现从5至35℃的温度增加增加了反应速率,其对应于38.5kJ.mol(-1)的活化能量。外推到大气条件允许结论是,温度与大气范围内的烟灰颗粒的CCN活化的O-3浓度同样重要。

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